This FAIRsharing record describes: The CHD7 database contains locus-specific, anonymised mutation data on both published and unpublished variants of the CHD7 gene related to the CHARGE syndrome pheno
All genes with a discovery nominal P<1×10−3 that also replicated in a dataset of a different disease (see main text). The table mirrors Table 2, with the only difference being whether replication is i
Objective To explore the causal relationship between peripheral blood cell levels (total white blood cells, neutrophils, monocytes, basophils, eosinophils, lymphocytes) and IgA nephropathy, and to pro
